SNP Report

Basic Info

Name	rs255097 dbSNP Ensembl
Location	chr7:30687343 - 30687343(1)
Variant Alleles	G/A/C
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.396565
Functional Annotation	intron_variant; NMD_transcript_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	intron_variant(ENST00000341843, ENST00000348438, ENST00000423776, ENST00000445981, ENST00000452278, ENST00000462882); NMD_transcript_variant(ENST00000423776, ENST00000452278); non_coding_transcript_variant(ENST00000462882); upstream_gene_variant(ENST00000471646, ENST00000506074)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
CRHR2	corticotropin releasing hormone receptor 2	7p14.3	3(2/1/0)

SNPs in LD with rs255097 (count: 0) View in gBrowse (chr7:30687343..30687343 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)